Canonical Allele Identifier: CA1335316799
Gene: CHRNG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541567C= , CM000664.2:g.232541567C= GRCh38
NC_000002.11:g.233406277C= , CM000664.1:g.233406277C= GRCh37
NC_000002.10:g.233114521C= NCBI36
NG_012954.1:g.6841C=
NG_012954.2:g.6876C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.506+38C= MANE Select ENSP00000498757.1:n.506+38C=
ENST00000389492.3:c.351-856C= ENSP00000374143.3:n.351-856C=
ENST00000389494.7:c.506+38C= ENSP00000374145.3:n.506+38C=
ENST00000485094.1:n.565C=
NM_005199.4:c.506+38C= NP_005190.4:n.506+38C=
NM_005199.5:c.506+38C= MANE Select NP_005190.4:n.506+38C=